Canonical Allele Identifier: CA324069736
Gene: SSTR3 HGNC NCBI

Linked Data

dbSNP Id: rs772739627
gnomAD v2: 22-37613293-C-T
gnomAD v3: 22-37217253-C-T
gnomAD v4: 22-37217253-C-T
MyVariant Identifiers: chr22:g.37613293C>T (hg19) chr22:g.37217253C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37217253C>T , CM000684.2:g.37217253C>T GRCh38
NC_000022.10:g.37613293C>T , CM000684.1:g.37613293C>T GRCh37
NC_000022.9:g.35943239C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_005261721.3:c.-37+3154G>A XP_005261778.1:n.-37+3154G>A
XM_011530349.1:c.-694-1365G>A XP_011528651.1:n.-694-1365G>A
XM_005261721.4:c.-37+3154G>A XP_005261778.1:n.-37+3154G>A
XM_011530349.2:c.-694-1365G>A XP_011528651.1:n.-694-1365G>A
XM_017028924.1:c.-437-1365G>A XP_016884413.1:n.-437-1365G>A
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